Heparin/heparan sulfate analysis by covalently modified reverse polarity capillary zone electrophoresis-mass spectrometry

•Reverse polarity CE-MS enables the analysis of sulfated GAG mixtures.•Covalent neutral and cation coatings produce fast and reproducible separations.•The separation of oligosaccharides from tetra- to dodecasaccharides is demonstrated.•Structures with sulfation position and epimeric structural diffe...

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Bibliographic Details
Published in:Journal of Chromatography A 2018-04, Vol.1545, p.75-83
Main Authors: Sanderson, Patience, Stickney, Morgan, Leach, Franklin E., Xia, Qiangwei, Yu, Yanlei, Zhang, Fuming, Linhardt, Robert J., Amster, I. Jonathan
Format: Article
Language:English
Subjects:
Capillary zone electrophoresis
Covalent capillary coating
Mass spectrometry
Mixture analysis
Reverse polarity
Sulfated glycosaminoglycan
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Summary:•Reverse polarity CE-MS enables the analysis of sulfated GAG mixtures.•Covalent neutral and cation coatings produce fast and reproducible separations.•The separation of oligosaccharides from tetra- to dodecasaccharides is demonstrated.•Structures with sulfation position and epimeric structural differences are resolved.•More than 80 molecular compositions are determined from complex GAG mixture. Reverse polarity capillary zone electrophoresis coupled to negative ion mode mass spectrometry (CZE-MS) is shown to be an effective and sensitive tool for the analysis of glycosaminoglycan mixtures. Covalent modification of the inner wall of the separation capillary with neutral or cationic reagents produces a stable and durable surface that provides reproducible separations. By combining CZE-MS with a cation-coated capillary and a sheath flow interface, a rapid and reliable method has been developed for the analysis of sulfated oligosaccharides from dp4 to dp12. Several different mixtures have been separated and detected by mass spectrometry. The mixtures were selected to test the capability of this approach to resolve subtle differences in structure, such as sulfation position and epimeric variation of the uronic acid. The system was applied to a complex mixture of heparin/heparan sulfate oligosaccharides varying in chain length from dp3 to dp12 and more than 80 molecular compositions were identified by accurate mass measurement.
ISSN:0021-9673
1873-3778
DOI:10.1016/j.chroma.2018.02.052